| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203816266-203816666 | Common:3; Rare:140 | ||||
| chr2:203933980-203934440 | Common:1; Rare:58 | ||||
| chr2:204012070-204012540 | Common:4; Rare:123 | ||||
| chr2:204109610-204110020 | Common:2; Rare:124 | ||||
| chr2:204343700-204343990 | Common:2; Rare:46 | ||||
| chr2:205771140-205771600 | Common:4; Rare:94 | ||||
| chr2:206084255-206084713 | Common:11; Rare:154 | ||||
| chr2:206085010-206085359 | Common:2; Rare:214 | ||||
| chr2:206146797-206147769 | Common:6; Rare:308; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:207163378-207163813 | Common:2; Rare:151 | ||||
| chr2:207395010-207395280 | Common:1; Rare:63 | ||||
| chr2:207530680-207531214 | Rare:251 | ||||
| chr2:207636956-207637441 | Common:2; Rare:163 | ||||
| chr2:207796560-207796840 | Common:3; Rare:47 | ||||
| chr2:207796860-207797190 | Rare:73 |